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FDA 510(k)

KOPAN'S TARGET

K-Number: K915417 · 1992-01-14

ApplicantMedical Device Technologies, Inc.
Decision Date1992-01-14
Product CodeGAA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

KOPAN'S TARGET is the device name listed in this FDA 510(k) record. The listed applicant is Medical Device Technologies, Inc.. It received FDA 510(k) clearance on 1992-01-14 under 510(k) number K915417. The device is classified under product code GAA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KOPAN'S TARGET?

KOPAN'S TARGET is a medical device that received FDA 510(k) clearance on 1992-01-14. The listed applicant is Medical Device Technologies, Inc.. The 510(k) number is K915417.

When did KOPAN'S TARGET receive FDA 510(k) clearance?

KOPAN'S TARGET received FDA 510(k) clearance on 1992-01-14, under 510(k) number K915417.

Who is the listed applicant for KOPAN'S TARGET?

The FDA 510(k) record lists Medical Device Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KOPAN'S TARGET?

The FDA product code for KOPAN'S TARGET is GAA.

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Related Devices (Code: GAA)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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